Product NDC: | 68016-490 |
Proprietary Name: | Day-Time Night-Time |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Active Ingredient(s): | & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68016-490 |
Labeler Name: | Chain Drug Consortium, LLC (Premier Value) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100712 |
Package NDC: | 68016-490-40 |
Package Description: | 1 KIT in 1 CARTON (68016-490-40) * 10 CAPSULE in 1 BLISTER PACK * 10 CAPSULE in 1 BLISTER PACK |
NDC Code | 68016-490-40 |
Proprietary Name | Day-Time Night-Time |
Package Description | 1 KIT in 1 CARTON (68016-490-40) * 10 CAPSULE in 1 BLISTER PACK * 10 CAPSULE in 1 BLISTER PACK |
Product NDC | 68016-490 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100712 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Chain Drug Consortium, LLC (Premier Value) |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |